FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MEDIA CULTURE SYSTEM

K Number: K040530 · Decision Jun 25, 2004
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
258
Applicant Total
24
Review Days
116

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Basic Information

Device Name
MEDIA CULTURE SYSTEM
K Number
K040530
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.6180
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
<Genx> Intl., Inc.
Date Received
March 1, 2004
Decision Date
June 25, 2004
Product Code
MQL
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MQL Media, Reproductive

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQL), ordered by most recent decision date.

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Other Clearances by <Genx> Intl., Inc.

K Number Device Name
K112083 LIFEGLOBAL TOTAL, TOTAL FOR FERTILIZATION, TOTAL W/HEPES, HTF TOTAL, HTF TOTAL W/HEPES
K080395 SUNIVF DISHES
K053552 GLOBAL FERTILIZATION, EMBRYO CULTURE AND TRANSFER MEDIA
K053551 MICROMANIPULATION MEDIA SYSTEM, LG HYALURONIDASE AND LG PARAFFIN OIL
K023033 ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM)
K022590 PVP (POLYVINYLPYRROLIDONE)
K022352 HTF PLUS WITH HEPES (HTF WITH NON-ESSENTIAL AMINO ACIDS)
K022547 ACIDIFIED TYRODES SOLUTION
K022334 HTF PLUS - HTF WITH NON-ESSENTIAL AMINO ACIDS
K022330 ALLGRAD 45 AND 90 CELL SEPARATION MEDIA
Search all 24 clearances from <Genx> Intl., Inc. →